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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1529331생성일: 2026년 10월 24일

Dichloromethane → 6-(2,6-Difluorophenyl)-2-methyl-3-nitropyridine

https://huagongshe.com/ko/reaction/1529331

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물2,6-Difluorophenylboronic acidHCID 2734336—
반응물6-Bromo-2-methyl-3-nitropyridineHCID 24728014—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매Ethyl AcetateHCID 8857—
용매Sodium CarbonateHCID 10340—
용매1,4-DioxaneHCID 31275—
생성물6-(2,6-Difluorophenyl)-2-methyl-3-nitropyridineHCID 6795823556%

반응 조건

온도100 °C

반응 단계

A suspension of 2-bromo-6-methyl-5-nitropyridine (3 g, 13.82 mmol, Matrix Scientific), 2,6-difluorobenzeneboronic acid (4.37 g, 27.6 mmol, Alfa Aesar) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with DCM (0.564 g, 0.691 mmol, Strem) in Dioxane (60 mL) (degassed with argon for 30 min) and Na2CO3, 2.0 M (20.74 mL, 41.5 mmol) was heated to 100° C. under N2. After 3 h, 2,6-difluorobenzeneboronic acid (4.37 g, 27.6 mmol) was further added. After a total of 7 h, 2,6-difluorobenzeneboronic acid (2.18 g, 13.8 mmol) was further added. After a total of 9 h, the reaction mixture was cooled to 23° C., diluted with EtOAc (400 ml) and washed with brine (200 mL), dried over MgSO4, concentrated in vacuo and purified by silica gel chromatography (eluent: 5-10% EtOAc/hexane), affording 6-(2,6-difluorophenyl)-2-methyl-3-nitropyridine (1.931 g, 56%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09090593B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-07ddec78a2fc438a849269ed09293510
출처 메모uspto-grants-2015_07